1122-12-9 | 3,4-Dibromofuran-2,5-dione

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$13.00	$9.00
1g	95%	in stock	$34.00	$24.00
5g	95%	in stock	$149.00	$105.00
10g	95%	in stock	$289.00	$203.00
25g	95%	in stock	$491.00	$344.00

Description

• Catalog Number: AB50558
• Chemical Name: 3,4-Dibromofuran-2,5-dione
• CAS Number: 1122-12-9
• Molecular Formula: C4Br2O3
• Molecular Weight: 255.8490
• MDL Number: MFCD00030673
• SMILES: O=C1OC(=O)C(=C1Br)Br
• NSC Number: 94974

Computed Properties

• Complexity: 196
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 3
• XLogP3: 1.7

Upstream Synthesis Route

As a professional chemist, I will provide an in-depth look at the application of 3,4-Dibromofuran-2,5-dione in chemical synthesis.3,4-Dibromofuran-2,5-dione is a valuable building block in organic chemistry due to its versatile reactivity and unique structure. One of its key applications is as a diene in Diels-Alder reactions, where it serves as a precursor for the synthesis of various heterocyclic compounds. By reacting 3,4-Dibromofuran-2,5-dione with dienophiles under appropriate conditions, chemists can efficiently construct complex ring structures with high regio- and stereo-selectivity.Furthermore, 3,4-Dibromofuran-2,5-dione can also act as a useful electrophile in Friedel-Crafts reactions, allowing for the introduction of bromine functionalities onto aromatic rings. This enables the synthesis of brominated aromatic compounds that are important intermediates in the production of pharmaceuticals, agrochemicals, and materials science.Additionally, the presence of two bromine atoms in the furan ring of 3,4-Dibromofuran-2,5-dione enhances its nucleophilicity and electrophilicity, making it a valuable reagent for various carbon-carbon and carbon-heteroatom bond-forming reactions. Its ability to undergo diverse transformations under mild reaction conditions makes it a valuable tool for the synthesis of structurally diverse and biologically active molecules.In conclusion, the unique properties of 3,4-Dibromofuran-2,5-dione make it a versatile and valuable compound in chemical synthesis, enabling the construction of complex heterocyclic and aromatic structures with high efficiency and selectivity.

Literature

• Bromomaleimide-linked bioconjugates are cleavable in mammalian cells.

  Chembiochem : a European journal of chemical biology 20120102